12,426 variants MyGeneLog™ checks for — each with its own plain-language page and cited source. New findings are collected from the public GWAS Catalog every twenty minutes.
ST6GAL1 · rs11710456
See detailed info → Standard on its ownPDE4D · rs159497
See detailed info → Standard on its ownTBX15 · rs17023457
See detailed info → StandardRECK · rs4878639
See detailed info → Standard on its ownKCNJ16 · rs312691
See detailed info → StandardCD44 · rs10768122
See detailed info → Standard on its ownJMJD1C · rs7923609
See detailed info → StandardABCG2 · rs1481012
See detailed info → StandardSLC45A3 · rs12409639
See detailed info → StandardSLC2A9 · rs4475146
See detailed info → StandardPYGL · rs7142143
See detailed info → StandardEXOC3L2 · rs17356664
See detailed info → Standard on its ownHBB · rs7950726
See detailed info → Standard on its ownSHBG · rs72829446
See detailed info → Standardnear VRK2 · rs13026414
See detailed info → StandardF13A1 · rs3024321
See detailed info → StandardF7/F10 · rs2181540
See detailed info → Standard on its ownLIN28B · rs17065417
See detailed info → Standard on its ownHACE1 · rs4336470
See detailed info → StandardNOX4 · rs7130284
See detailed info →Showing 20 of 12426 · page 539 of 622
One specific position in the genome (an rsID), explained in plain language with what published research has found it linked to, and how strong that link actually is.
The public GWAS Catalog, checked every twenty minutes, plus variants added manually after research review. Every one passes the same quality gate before publishing.
No. Listing reflects an association from published research, not a diagnosis or a cause. Most common variants shift probability modestly rather than determining an outcome.
Yes — the search box above matches gene symbols and rsIDs as well as trait names.